Accelevir provides targeted short-read NGS and long-read sequencing for therapeutic vector characterization, CRISPR off-target mapping, and AAV genome integrity analysis. Our platforms combine base-level accuracy with the ability to resolve large structural variations.
Capabilities:
- Short-read NGS for variant detection, quantification, and allele frequency analysis.
- Long-read sequencing for structural variant mapping, integration site profiling, and vector genome stability.
- Custom target enrichment to boost sensitivity in low-abundance samples.
- Bioinformatics pipelines for viral vectors, edited genomes, and pathogen sequencing.
Applications:
- On/off-target CRISPR sequencing.
- AAV genome integrity QC.
- Viral diversity and quasispecies analysis.
- Integration site mapping for safety assessment.